25 research outputs found

    PREVALANCE, CLINICAL CHARACTERISTICS, POSSIBLE ETIOLOGICALAND DIAGNOSTIC APPROACH IN DOGS WITH ACRAL LICK DERMATITIS

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    Acral lick dermatitis (ALD) is a chronic irritating skin disease in dogs caused by excessive licking of specified skin areas. The objective of the present study was to investigate the clinical characteristics and diagnostic approach and to classify the possible etiologies of ALD in dogs. Case investigation forALD included a recording of thorough history presenting, clinical signs and signs associated with the lesion, laboratory and orthopedic investigations, cytological examination, and biopsy/histopathology and hematology. Among the dermatological cases, the overall prevalence of ALD was 7.27%. Prevalence of ALD was higher in young (1-3years) age group dogs predominantly in male dogs during winter months with temperature <200C and Labrador retriever was the most commonly affected breed. Possible etiologies in 30 cases diagnosed with ALD were psychogenic triggers (19 cases, 63.33%) followed by only organic triggers (9 cases, 30%) and a combination of primary organic triggers with perpetuating psychogenic triggers (2 cases, 6.66%). The left forelimb (40%) followed by the right forelimb (13.33%) were the most affected limbs with ALD. Lesion characteristics observed were alopecia in 27 dogs (90%), circumscribed lesions in 16 dogs (53.33%), induration and firmness in 15 dogs (50%), ulceration in 14 dogs (46.66%), and moist lesions in 14 dogs (46.66%). The most common clinical signs associated with the disease were licking of paws in both organic and psychogenic triggers and additionally pruritus and erythema. Cytological examination of the lesions revealed chronic active inflammation in 24 cases and purulent inflammation in 6 cases. Histopathological findings of ALD lesion illustrated hyperkeratosis, acanthosis, and dermal fibrosis with vertical streaking. Stress polycythemia was a consistent finding recorded with only psychogenic triggers

    A Systematic Review and Comparative Meta-analysis of Non-destructive Fruit Maturity Detection Techniques

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    The global fruit industry is growing rapidly due to increased awareness of the health benefits associated with fruit consumption. Fruit maturity detection plays a crucial role in fruit logistics and maintenance, enabling farmers and fruit industries to grade fruits and develop sustainable policies for enhanced profitability and service quality. Non-destructive fruit maturity detection methods have gained significant attention, especially with advancements in machine vision and spectroscopic techniques. This systematic review provides a concise overview of the techniques and algorithms used in fruit quality grading by farmers and industries. The study reviewed 63 full-text articles published between 2012 and 2023 along with their bibliometric analysis. Qualitative analysis revealed that researchers from various disciplines contributed to this field, with techniques falling into 3 categories: machine vision (mathematical modelling or deep learning), spectroscopy and other miscellaneous approaches. There was a high level of diversity among these categories, as indicated by an I-square value of 88.37% in the heterogeneity analysis. Meta-analysis, using odds ratios as the effect measure, established the relationship between techniques and their accuracy. Machine vision showed a positive correlation with accuracy across different categories. Additionally, Egger's and Begg's tests were used to assess publication bias and no strong evidence of its occurrence was found. This study offers valuable insights into the advantages and limitations of various fruit maturity detection techniques. For employing statistical and meta-analytical methods, key factors such as accuracy and sample size have been considered. These findings will aid in the development of effective strategies for fruit quality assessment

    The malleable brain: plasticity of neural circuits and behavior: A review from students to students

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    One of the most intriguing features of the brain is its ability to be malleable, allowing it to adapt continually to changes in the environment. Specific neuronal activity patterns drive long-lasting increases or decreases in the strength of synaptic connections, referred to as long-term potentiation (LTP) and long-term depression (LTD) respectively. Such phenomena have been described in a variety of model organisms, which are used to study molecular, structural, and functional aspects of synaptic plasticity. This review originated from the first International Society for Neurochemistry (ISN) and Journal of Neurochemistry (JNC) Flagship School held in Alpbach, Austria (Sep 2016), and will use its curriculum and discussions as a framework to review some of the current knowledge in the field of synaptic plasticity. First, we describe the role of plasticity during development and the persistent changes of neural circuitry occurring when sensory input is altered during critical developmental stages. We then outline the signaling cascades resulting in the synthesis of new plasticity-related proteins, which ultimately enable sustained changes in synaptic strength. Going beyond the traditional understanding of synaptic plasticity conceptualized by LTP and LTD, we discuss system-wide modifications and recently unveiled homeostatic mechanisms, such as synaptic scaling. Finally, we describe the neural circuits and synaptic plasticity mechanisms driving associative memory and motor learning. Evidence summarized in this review provides a current view of synaptic plasticity in its various forms, offers new insights into the underlying mechanisms and behavioral relevance, and provides directions for future research in the field of synaptic plasticity.Fil: Schaefer, Natascha. University of Wuerzburg; AlemaniaFil: Rotermund, Carola. University of Tuebingen; AlemaniaFil: Blumrich, Eva Maria. Universitat Bremen; AlemaniaFil: Lourenco, Mychael V.. Universidade Federal do Rio de Janeiro; BrasilFil: Joshi, Pooja. Robert Debre Hospital; FranciaFil: Hegemann, Regina U.. University of Otago; Nueva ZelandaFil: Jamwal, Sumit. ISF College of Pharmacy; IndiaFil: Ali, Nilufar. Augusta University; Estados UnidosFil: García Romero, Ezra Michelet. Universidad Veracruzana; MéxicoFil: Sharma, Sorabh. Birla Institute of Technology and Science; IndiaFil: Ghosh, Shampa. Indian Council of Medical Research; IndiaFil: Sinha, Jitendra K.. Indian Council of Medical Research; IndiaFil: Loke, Hannah. Hudson Institute of Medical Research; AustraliaFil: Jain, Vishal. Defence Institute of Physiology and Allied Sciences; IndiaFil: Lepeta, Katarzyna. Polish Academy of Sciences; ArgentinaFil: Salamian, Ahmad. Polish Academy of Sciences; ArgentinaFil: Sharma, Mahima. Polish Academy of Sciences; ArgentinaFil: Golpich, Mojtaba. University Kebangsaan Malaysia Medical Centre; MalasiaFil: Nawrotek, Katarzyna. University Of Lodz; ArgentinaFil: Paid, Ramesh K.. Indian Institute of Chemical Biology; IndiaFil: Shahidzadeh, Sheila M.. Syracuse University; Estados UnidosFil: Piermartiri, Tetsade. Universidade Federal de Santa Catarina; BrasilFil: Amini, Elham. University Kebangsaan Malaysia Medical Centre; MalasiaFil: Pastor, Verónica. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia ; ArgentinaFil: Wilson, Yvette. University of Melbourne; AustraliaFil: Adeniyi, Philip A.. Afe Babalola University; NigeriaFil: Datusalia, Ashok K.. National Brain Research Centre; IndiaFil: Vafadari, Benham. Polish Academy of Sciences; ArgentinaFil: Saini, Vedangana. University of Nebraska; Estados UnidosFil: Suárez Pozos, Edna. Instituto Politécnico Nacional; MéxicoFil: Kushwah, Neetu. Defence Institute of Physiology and Allied Sciences; IndiaFil: Fontanet, Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia ; ArgentinaFil: Turner, Anthony J.. University of Leeds; Reino Unid

    Mycobacterium tuberculosis Transcriptional Adaptation, Growth Arrest and Dormancy Phenotype Development Is Triggered by Vitamin C

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    BACKGROUND: Tubercle bacilli are thought to persist in a dormant state during latent tuberculosis (TB) infection. Although little is known about the host factors that induce and maintain Mycobacterium tuberculosis (M. tb) within latent lesions, O(2) depletion, nutrient limitation and acidification are some of the stresses implicated in bacterial dormancy development/growth arrest. Adaptation to hypoxia and exposure to NO/CO is implemented through the DevRS/DosT two-component system which induces the dormancy regulon. METHODOLOGY/PRINCIPAL FINDINGS: Here we show that vitamin C (ascorbic acid/AA) can serve as an additional signal to induce the DevR regulon. Physiological levels of AA scavenge O(2) and rapidly induce the DevR regulon at an estimated O(2) saturation of <30%. The kinetics and magnitude of the response suggests an initial involvement of DosT and a sustained DevS-mediated response during bacterial adaptation to increasing hypoxia. In addition to inducing DevR regulon mechanisms, vitamin C induces the expression of selected genes previously shown to be responsive to low pH and oxidative stress, triggers bacterial growth arrest and promotes dormancy phenotype development in M. tb grown in axenic culture and intracellularly in THP-1 cells. CONCLUSIONS/SIGNIFICANCE: Vitamin C mimics multiple intracellular stresses and has wide-ranging regulatory effects on gene expression and physiology of M. tb which leads to growth arrest and a 'dormant' drug-tolerant phenotype, but in a manner independent of the DevRS/DosT system. The 'AA-dormancy infection model' offers a potential alternative to other models of non-replicating persistence of M. tb and may be useful for investigating host-'dormant' M. tb interactions. Our findings offer a new perspective on the role of nutritional factors in TB and suggest a possible role for vitamin C in TB

    ISSN 2347-954X (Print) Three-Dimensional Sono hystero salpingography: A Diagnostic Tool in Evolution of Infertility Cases

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    Abstract: Infertility is the most common health concern in young adults. The aim is to study the diagnostic role of3-Dimensional sono hystero salpingography for detection of intrauterine lesions, extra uterine lesions and tubal pathology. It is a hospital based prospective, descriptive study in which50 patients with normal uterine cavity at transvaginal ultrasound underwent infertility workup at our outpatient clinic. All patients underwent 3-Dimensional sono hystero salpingography. These were then subjected to diagnostic hysterolaparoscopy the following day. The results of both were compared and correlated. Sensitivity, Specificity, Positive predictive value (PPV), Negative predictive value (NPV) and accuracy of 3-Dimensional sono hystero salpingography was compared with diagnostic hystero laparoscopy in detecting intrauterine, extra uterine lesions and tubal patency. The sensitivity, specificity, PPV, NPV and accuracy of 3-Dimensional sono hystero salpingography was 71.4%, 100%, 100%, 95.58% and 96% respectively for detecting intrauterine lesions; was 90.91%, 92.3%, 79.9%, 97.3% and 92% for detecting ovarian pathology; and 97.6%, 87.5%, 97.6%, 87.5% and 96% for detecting tubal patency. For diagnostic hystero laparoscopy, considered as the gold standard, the sensitivity, specificity, PPV, NPV and accuracy was 100%. It was concluded that the diagnostic value of 3-Dimensional sono hystero salpingography is comparable to diagnostic hystero laparoscopy in detecting intrauterine lesions, extra uterine lesions and tubal patency. Thus 3-D SHSG should be included as a preliminary investigation in infertility work up in women with normal uterine cavity in transvaginal ultrasound. Keywords: 3Dimensional sono hystero salpingography, diagnostic hystero laparoscopy, intrauterine lesions, tubal patency, ovarian pathology

    Image1_Sirtuin1 meditated modification of Notch1 intracellular domain regulates nucleolar localization and activation of distinct signaling cascades.pdf

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    Notch signaling is involved in cell fate decisions in the development and maintenance of tissue homeostasis. Spatial regulation of the Notch1 intracellular domain (NIC1), has been shown to underpin signaling outcomes mediated by this receptor. We recently reported a putative Nucleolar Localization Sequence (NoLS) in NIC1. Here we investigate if the putative NoLS identified in NIC1 regulates localization in the nucleolus and anti-apoptotic activity. Confocal imaging of live cells expressing NIC1 or forms modified by deletion or site-directed mutagenesis established that the putative NoLS in NIC1 is required for nucleolar localization and regulated by the deacetylase Sirtuin1. Subsequent analysis of anti-apoptotic activity revealed signaling cascades linked to nucleolar localization. For this, etoposide and 4-Nitroquinoline 1-oxide, an inhibitor of topoisomerase-II and a UV mimetic drug respectively, were used as prototypic triggers of genomic damage in a mammalian cell line. While NIC1 blocked apoptosis regardless of its localization to the nucleoplasm or nucleolus, modifications of NIC1 which promoted localization to the nucleolus triggered a dependence on the nucleolar proteins fibrillarin and nucleolin for anti-apoptotic activity. Further, cells co-expressing NIC1 and Sirtuin1 (but not its catalytically inactive form), confirmed both spatial regulation and the switch to dependence on the nucleolar proteins. Finally, site-directed mutagenesis showed that the NoLS lysine residues are targets of Sirtuin1 activity. NIC1 mediated transcription is not similarly regulated. Thus, NIC1 localization to the nucleolus is regulated by Sirtuin1 modification of the lysine residues in NoLS and triggers a distinct signaling cascade involving nucleolar intermediates for anti-apoptotic activity.</p

    Electric Field-Driven Spatial Information Capture of Dissipative Biocondensate States

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    The theory behind origin of life to Darwinian evolution considers emergence of dissipative structures driven by the flow of energy across all length scales. To this end, developing and deeper understanding of non-equilibrium self-assembly processes under continuous supply of energy is a demanding matter, both in fundamental and application (for e.g. developing dynamic materials) viewpoint. Herein, we demonstrate transient self-assembly of a DNA-histone condensate where trypsin (already present in the system) hydrolyse histone resulting disassembly. As the process is short-lived, the information of intermediate states between complete assembly and disassembly remains uncaptured in absence of any external energy. We show that performing the process under electric field of varying strength results fractionation of myriad of short-lived states which appears as band in different zone. Deconvolution and capturing of many hidden self-assembling species of similar components but of different compositions which otherwise never be formed in absence of electric energy, will be of immense importance in applied non-equilibrium thermodynamics

    Evaluation of Observed and Future Climate Change Projection for Uttarakhand, India, Using CORDEX-SA

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    The climate change scenarios, especially global warming, have raised significant concerns, and the Himalayan regions such as Uttarakhand are highly vulnerable to such climatic shifts. Considering 10 Coordinated Regional Climate Downscaling Experiments in South Asia (CORDEX-SA), experiments with 3 regional climate models (RCMs), driven by 13 global climate models, historical estimates and future projections are analyzed from the mid-century (MC) i.e., from 2021–2050 to the end of the century (EC) i.e., from 2070–2099 to characterize annual and seasonal variations in precipitation and temperature. The analysis shows a decrease in the annual average precipitation by 5.92% at MC and an increase of 5.97% at EC for the Representative Climate Pathway (RCP) 4.5, while precipitation may likely increase from 2.83% to 15.89% towards MC and EC in the RCP 8.5. The maximum temperature may likely increase from 0.42 °C to 3.07 °C from MC to EC in the RCP 4.5 and from 0.83 °C to 5.49 °C in the RCP 8.5. In addition, the minimum temperature may increase from 0.80 °C to 3.25 °C from MC to EC in the RCP 4.5 and from 0.30 °C to 5.86 °C from MC to EC in the RCP 8.5. Notably, a decrease in the pre-monsoon precipitation at EC and a higher increase in the maximum temperature during the monsoon season are observed. An increase in the maximum temperature along with precipitation may lead to an increase in the frequency of the monsoon season’s extreme rainfall events

    Small ncRNA Expression-Profiling of Blood from Hemophilia A Patients Identifies miR-1246 as a Potential Regulator of Factor 8 Gene.

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    Hemophilia A (HA) is a bleeding disorder caused by deficiency of functional plasma clotting factor VIII (FVIII). Genetic mutations in the gene encoding FVIII (F8) have been extensively studied. Over a thousand different mutations have been reported in the F8 gene. These span a diverse range of mutation types, namely, missense, splice-site, deletions of single and multiple exons, inversions, etc. There is nonetheless evidence that other molecular mechanisms, in addition to mutations in the gene encoding the FVIII protein, may be involved in the pathobiology of HA. In this study, global small ncRNA expression profiling analysis of whole blood from HA patients, and controls, was performed using high-throughput ncRNA microarrays. Patients were further sub-divided into those that developed neutralizing-anti-FVIII antibodies (inhibitors) and those that did not. Selected differentially expressed ncRNAs were validated by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) analysis. We identified several ncRNAs, and among them hsa-miR-1246 was significantly up-regulated in HA patients. In addition, miR-1246 showed a six-fold higher expression in HA patients without inhibitors. We have identified an miR-1246 target site in the noncoding region of F8 mRNA and were able to confirm the suppressory role of hsa-miR-1246 on F8 expression in a stable lymphoblastoid cell line expressing FVIII. These findings suggest several testable hypotheses vis-Ă -vis the role of nc-RNAs in the regulation of F8 expression. These hypotheses have not been exhaustively tested in this study as they require carefully curated clinical samples
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